Ibuprofen
This medicine should always be taken exactly as described in this patient leaflet or as directed by a doctor or pharmacist.
used for
Ibufen for children FORTE with strawberry flavor belongs to a group of nonsteroidal anti-inflammatory drugs (NSAIDs). The medicine has analgesic, antipyretic, and anti-inflammatory effects.
The medicine is intended for use in children, adolescents, and adults in the following cases:
strawberry flavor
Before starting treatment with Ibufen for children FORTE with strawberry flavor, the patient should discuss it with their doctor or pharmacist.
During treatment with ibuprofen, symptoms of allergic reactions to this medicine have been reported, including difficulty breathing, facial and neck edema (angioedema), and chest pain. If the patient notices any of these symptoms, they should stop taking Ibufen for children FORTE with strawberry flavor and contact their doctor or emergency services immediately.
The patient should inform their pharmacist or doctor if they have an infection - see below, section "Infections".
Taking anti-inflammatory/pain-relieving medications, such as ibuprofen, may be associated with a small increased risk of heart attack or stroke, especially when taken in high doses. Do not exceed the recommended dose and duration of treatment.
Before taking Ibufen for children FORTE with strawberry flavor, the patient should discuss treatment with their doctor or pharmacist if:
The patient should also consult their doctor if they are taking other medicines, especially blood-thinning medicines, diuretics, cardiac glycosides, corticosteroids (see section "Ibufen for children FORTE with strawberry flavor and other medicines").
The patient should avoid taking ibuprofen with other NSAIDs, including selective cyclooxygenase-2 inhibitors, due to the increased risk of adverse reactions (see section "Ibufen for children FORTE with strawberry flavor and other medicines").
Taking the medicine in the smallest effective dose for the shortest duration necessary to relieve symptoms reduces the risk of adverse reactions. Elderly patients are more likely to experience adverse reactions.
There is a risk of gastrointestinal bleeding, ulceration, or perforation, which can be fatal and does not necessarily have to be preceded by warning signs or may occur in patients who have had such warning signs. If gastrointestinal bleeding or ulceration occurs, the medicine should be stopped immediately. Patients with a history of gastrointestinal disease, especially the elderly, should inform their doctor about any unusual gastrointestinal symptoms (especially bleeding), especially during the initial treatment period.
Concomitant, long-term use of different pain-relieving medications may lead to kidney damage with a risk of kidney failure (analgesic nephropathy). This risk may increase in the case of physical exertion resulting in salt loss and dehydration.
Therefore, concomitant, long-term use of different pain-relieving medications should be avoided.
There is a risk of kidney function disorders in dehydrated children and adolescents.
Severe skin reactions
In connection with ibuprofen treatment, severe skin reactions have been reported, including exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP). The patient should stop taking Ibufen for children FORTE with strawberry flavor and seek medical attention immediately if they experience any symptoms associated with severe skin reactions described in section 4.
Infections
Ibufen for children FORTE with strawberry flavor may mask the symptoms of infection, such as fever and pain. As a result, Ibufen for children FORTE with strawberry flavor may delay the use of appropriate infection treatment and consequently lead to an increased risk of complications.
This has been observed in bacterial pneumonia and bacterial skin infections associated with chickenpox. If the patient is taking this medicine during an infection and the symptoms of the infection persist or worsen, they should consult their doctor immediately.
During ibuprofen treatment, single cases of toxic amblyopia (visual impairment) have been reported, so any vision disturbances should be reported to the doctor.
The patient should tell their doctor or pharmacist about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take.
Ibufen for children FORTE with strawberry flavor may affect the action of other medicines or other medicines may affect the action of Ibufen for children FORTE with strawberry flavor. For example:
Also, some other medicines may be affected or have an effect on treatment with Ibufen for children FORTE with strawberry flavor. Therefore, before taking Ibufen for children FORTE with strawberry flavor with other medicines, the patient should always consult their doctor or pharmacist.
The medicine should be taken after meals, with a large amount of fluid.
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor or pharmacist before taking this medicine.
Pregnancy
Ibufen for children FORTE with strawberry flavor should not be taken during the last three months of pregnancy, as it may harm the unborn child or cause complications during delivery. It may cause kidney and heart disorders in the unborn child.
It may affect the patient's and their child's tendency to bleed and may cause delayed or prolonged labor.
Ibufen for children FORTE with strawberry flavor should not be taken during the first six months of pregnancy, unless it is absolutely necessary and prescribed by a doctor. If treatment is necessary during this period or when trying to conceive, the smallest effective dose of the medicine should be used for the shortest possible time. Ibufen for children FORTE with strawberry flavor taken for a period longer than a few days, starting from the 20th week of pregnancy, may cause kidney disorders in the unborn child, leading to a low level of amniotic fluid surrounding the child (oligohydramnios) or narrowing of the arterial duct (ductus arteriosus) in the child's heart. If longer treatment is necessary, the doctor may recommend additional monitoring.
Breastfeeding
Ibuprofen passes into breast milk in small amounts, but it is very unlikely to have a negative effect on the breastfed infant.
Fertility
This medicine belongs to a group of medicines (nonsteroidal anti-inflammatory drugs) that may have a negative effect on female fertility. This effect is temporary and disappears after the end of treatment.
As large doses of Ibufen for children FORTE with strawberry flavor may cause adverse reactions related to the central nervous system, such as fatigue and dizziness, it may impair the ability to drive vehicles and operate machinery. This warning is particularly relevant when the medicine is taken with alcohol.
The medicine contains 2.4 g of liquid maltitol in each 5 ml of oral suspension. If the patient has previously been diagnosed with intolerance to some sugars, they should consult their doctor before taking the medicine.
The medicine contains 5 mg of sodium benzoate in each 5 ml of oral suspension.
The medicine contains less than 1 mmol (23 mg) of sodium in each 5 ml of oral suspension, which means the medicine is considered "sodium-free".
This medicine should always be taken exactly as described in this patient leaflet or as directed by a doctor or pharmacist. In case of doubt, the patient should consult their doctor or pharmacist.
The medicine should be taken orally.
A dosing device in the form of a syringe is included with the packaging for accurate dosing.
Before use, the bottle should be shaken.
When determining the dose of ibuprofen, the patient's body weight and age should be taken into account. The usual single dose of ibuprofen is 7-10 mg per kilogram of body weight, up to a maximum daily dose of 30 mg per kilogram of body weight, divided into 3-4 single doses.
The minimum interval between consecutive doses is 6 hours.
The patient should take the smallest effective dose for the shortest duration necessary to relieve symptoms and minimize the risk of adverse reactions. If the symptoms of the infection (such as fever and pain) persist or worsen, the patient should consult their doctor immediately (see section 2).
Do not exceed the maximum daily dose.
Recommended dose
Body weight (patient's age) | Single dose | Dosing frequency per day (maximum daily dose of ibuprofen) |
5-7.6 kg (3-6 months) | 1.25 ml (1 × 50 mg) | 3 times (150 mg) |
7.7-9 kg (6-12 months) | 1.25 ml (1 × 50 mg) | 3-4 times (150-200 mg) |
10-15 kg (1-3 years) | 2.5 ml (1 × 100 mg) | 3 times (300 mg) |
16-20 kg (4-6 years) | 3.75 ml (1 × 150 mg) | 3 times (450 mg) |
21-29 kg (7-9 years) | 5 ml (1 × 200 mg) | 3 times (600 mg) |
30-40 kg (10-12 years) | 7.5 ml (1 × 300 mg) | 3 times (900 mg) |
Above 40 kg (adolescents from 12 years and adults) | 5-10 ml (200-400 mg) | 3 times (1200 mg) |
In the case of children aged 3-5 months, the patient should consult their doctor if the symptoms worsen or do not improve after 24 hours.
In the case of children over 6 months, the patient should consult their doctor if the medicine needs to be given for more than 3 days or if the symptoms worsen.
The medicine is intended for short-term use.
The medicine should not be given to infants with a body weight below 5 kg.
In patients with mild and moderate kidney and/or liver function disorders, there is no need to reduce the dose of Ibufen for children FORTE with strawberry flavor.
In elderly patients, dose adjustment is not required.
If the patient has taken a higher dose of Ibufen for children FORTE with strawberry flavor than recommended or if a child has accidentally taken the medicine, they should always consult their doctor or go to the nearest hospital to get an opinion on possible health risks and advice on what to do.
Symptoms of overdose may include nausea, abdominal pain, vomiting (which may contain blood), gastrointestinal bleeding (see also section 4 below), diarrhea, headache, ringing in the ears, dizziness, and disorientation. They may also include agitation, drowsiness, disorientation, or coma. In rare cases, seizures may occur. After taking large doses, drowsiness, chest pain, palpitations, loss of consciousness, seizures (mainly in children), weakness, and dizziness have been reported. Additionally, the prothrombin time (INR) may be prolonged, probably due to the disruption of blood clotting factors. Acute kidney failure and liver damage may occur. In patients with asthma, worsening of asthma symptoms may occur.
Furthermore, low blood pressure and breathing difficulties may occur.
Overdose cases are rare. There is no specific antidote. Treatment is symptomatic and supportive. The doctor may consider administering activated charcoal if it has been less than one hour since the overdose.
Do not take a double dose to make up for a missed dose.
If the patient has any further doubts about taking this medicine, they should consult their doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The patient should stop taking ibuprofen and seek medical attention immediately if they experience any of the following symptoms:
Ibufen for children FORTE with strawberry flavor is generally well-tolerated.
During short-term use of ibuprofen in doses available without a prescription, the following adverse reactions have been observed.
Adverse reactions are ranked according to frequency of occurrence.
Common (occurring in less than 1 in 10 patients)
Uncommon (occurring in less than 1 in 100 patients)
Rare (occurring in less than 1 in 1,000 patients)
Very rare (occurring in less than 1 in 10,000 patients)
Frequency not known (frequency cannot be estimated from available data):
In individual cases, depression and psychotic reactions have been described.
If side effects occur, including those not listed in this leaflet, the patient should tell their doctor or pharmacist, or nurse. Side effects can be reported directly to the Department of Adverse Reaction Monitoring of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C
02-222 Warsaw
Phone: +48 22 49 21 301
Fax: +48 22 49 21 309
Website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
Reporting side effects will help gather more information on the safety of the medicine.
Store at a temperature below 25°C.
Store in the original packaging.
Store the bottle tightly closed.
The medicine should be stored out of sight and reach of children.
Do not use this medicine after the expiration date stated on the bottle and carton after:
EXP. The expiration date refers to the last day of the specified month.
The medicine is suitable for use for 6 months after the first opening of the bottle.
Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
The medicine is a white or almost white oral suspension with a strawberry flavor and smell.
Available packaging:
100 ml or 40 ml of oral suspension in a white PET bottle with an adapter inserted, closed with a polyethylene cap with a tamper-evident ring and a child-resistant closure system.
The bottle, together with the patient leaflet and a dosing device in the form of a syringe, is placed in a cardboard box. The dosing device in the form of a syringe has a volume of 5 ml and a scale every 0.25 ml.
Zakłady Farmaceutyczne POLPHARMA S.A.
ul. Pelplińska 19, 83-200 Starogard Gdański
phone: +48 22 364 61 01
Zakłady Farmaceutyczne POLPHARMA S.A.
Medana branch in Sieradz
ul. Władysława Łokietka 10, 98-200 Sieradz
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